Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT03944733

Iron Status, Maternal Depressive Symptoms, and Mother-child Interactions

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Penn State University · Academic / Other
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

This study aims to examine the relation between iron status and maternal-child interactions as well as maternal depressive symptoms in mothers from central Pennsylvania.

Detailed description

Investigators aim to follow mothers and their infants from 6 weeks to 6 months in the postpartum to understand the relation between iron status and mother-child interactions and depressive symptoms. During this period, iron deficient anemic mothers will receive an intervention with iron with the scope of improving iron status, reducing their depressive symptoms, and in turn, increasing the quality of parenting behaviors during mother-child interactions. The control group will be iron sufficient mothers who will receive a placebo.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTIron65 mg of iron (ferrous sulfate)
DIETARY_SUPPLEMENTGelatin600 mg gelatin

Timeline

Start date
2019-12-01
Primary completion
2020-12-30
Completion
2020-12-30
First posted
2019-05-09
Last updated
2025-11-20

Source: ClinicalTrials.gov record NCT03944733. Inclusion in this directory is not an endorsement.